Species-specific differences in DNA damage sensitivity at early developmental stage: A comparative study of sterlet (Acipenser ruthenus) and common carp (Cyprinus carpio)
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, srovnávací studie
PubMed
39019243
DOI
10.1016/j.etap.2024.104501
PII: S1382-6689(24)00141-8
Knihovny.cz E-zdroje
- Klíčová slova
- DNA repair, Development, Fish, Nuclear abnormality, Species-specific,
- MeSH
- apoptóza účinky léků MeSH
- chemické látky znečišťující vodu toxicita MeSH
- druhová specificita * MeSH
- embryo nesavčí * účinky léků MeSH
- fragmentace DNA MeSH
- kamptothecin * toxicita analogy a deriváty MeSH
- kapři * embryologie genetika MeSH
- mutageny toxicita MeSH
- nádorový supresorový protein p53 genetika metabolismus MeSH
- poškození DNA * MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- srovnávací studie MeSH
- Názvy látek
- chemické látky znečišťující vodu MeSH
- kamptothecin * MeSH
- mutageny MeSH
- nádorový supresorový protein p53 MeSH
DNA damage in embryos shapes the development of an organism. Understanding life stage-specific differences between fish species is essential for ecological risk assessment measures. We explored DNA damage sensitivity in two nonmodel fish species, sterlet (Acipenser ruthenus) and common carp (Cyprinus carpio). Embryos of these species were exposed to a model genotoxicant, camptothecin (CPT), during cleavage (2-cell) stage and gastrulation. Results revealed a species-specific DNA damage sensitivity only at cleavage stage. 3 nM CPT caused lethality in sterlet embryos while carp embryos hatched normally. Multiple nuclear abnormalities were observed in sterlet embryos by early gastrula stage. However, carp embryos exhibited nuclear abnormalities and DNA fragmentation at neurula stage only when exposed to 7 nM CPT. Moreover, increased expression of tp53 in carp embryos at gastrula stage suggests activation of apoptosis mechanism. These findings suggest that carp embryos activate DNA damage response more efficiently than sterlet embryos at same developmental stage.
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